6-Monodeoxy-6-monobromo-beta-cyclodextrin

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6-Monodeoxy-6-monobromo-beta-cyclodextrin
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6-Monodeoxy-6-monobromo-beta-cyclodextrin

Original price was: $1,795.00.Current price is: $895.00.

Catalog Number: B2027372 (100 mg)
6-Monodeoxy-6-monobromo-beta-cyclodextrin is a selectively modified cyclic oligosaccharide in which a single primary hydroxyl group at the C6 position is replaced with a bromine atom. This targeted halogen substitution provides a reactive site for further chemical functionalization through nucleophilic displacement while preserving the native toroid structure. It is commonly utilized as a versatile intermediate in custom synthesis to produce novel functionalized cyclodextrin derivatives for molecular recognition research. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (1 vote)

6-Monodeoxy-6-monobromo-beta-cyclodextrin
Catalog number: B2027372
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 100 mg
Molecular Weight or Concentration: 1197.9
Supplied as: Chemicals
Storage: 2-8 ËšC
Keywords: 6-Monobromo-6-monodeoxy-beta-cyclodextrin, 6-Bromo-6-deoxy-beta-cyclodextrin, 6-Monobromo-6-monodeoxy-β-cyclodextrin, 6-Bromo-6-deoxy-β-cyclodextrin

References:
1. Gadelle, A., & Defaye, J. (1991). Selective halogenation at C-6 of cyclodextrins. Angewandte Chemie International Edition in English, 30(1), 78-80.
2. Ashton, P. R., Ellwood, P., Staton, I., & Stoddart, J. F. (1991). Regioselective functionalization of cyclodextrins. Journal of the Chemical Society, Perkin Transactions 2, (9), 1497-1507.
3. Khan, A. R., Forgo, P., Stine, K. J., & D’Souza, V. T. (1998). Methods for selective modification of cyclodextrins. Chemical Reviews, 98(5), 1977-1996.
4. Rong, D., & D’Souza, V. T. (1990). A convenient method for the monomodification of β-cyclodextrin. Tetrahedron Letters, 31(30), 4275-4278.
5. Tang, W., & Ng, S. C. (2008). Substituted β-cyclodextrins: Synthesis and applications in chiral resolution. Journal of Chromatography A, 1204(1), 3-15.
6. Melton, L. D., & Slessor, K. N. (1971). Synthesis of monosubstituted cycloheptaamylose derivatives. Carbohydrate Research, 18(1), 29-37.
7. Boger, J., Corcoran, R. J., & Lehn, J. M. (1978). Cyclodextrin chemistry: Selective modification of primary hydroxyl groups. Helvetica Chimica Acta, 61(6), 2190-2218.
8. Takeo, K., Mitoh, H., & Uemura, K. (1989). Selective chemical modification of cyclomalto-oligosaccharides. Carbohydrate Research, 187(2), 203-221.
9. Guillo, F., Hamelin, B., Jullien, L., Canceill, J., & Lehn, J. M. (1995). Modification of cyclodextrins at the primary rim. Bulletin de la Société Chimique de France, 132, 857-866.
10. Szejtli, J. (1998). Introduction and general overview of cyclodextrin chemistry. Chemical Reviews, 98(5), 1743-1754.
6-Monodeoxy-6-monobromo-beta-cyclodextrin

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Additional Information

Weight 0.15 oz
Dimensions 2 × 0.5 × 0.5 in
5/5 - (1 vote)

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